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Pathogens and Disease|June 23, 2017
Multi-target activity of Hemidesmus indicus decoction against innovative HIV-1 drug targets and characterization of Lupeol mode of actionFrancesca Esposito, Manuela Mandrone, Claudia Del Vecchio, et al.
European Journal of Medicinal Chemistry|October 21, 2018
Novel natural non-nucleoside inhibitors of HIV-1 reverse transcriptase identified by shape- and structure-based virtual screening techniquesGiosuè Costa, Roberta Rocca, Angela Corona, et al.
Molecules (Basel, Switzerland)|July 2, 2021
Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated FunctionsRita Meleddu, Angela Corona, Simona Distinto, et al.
Antiviral Research|January 23, 2022
Cynarin blocks Ebola virus replication by counteracting VP35 inhibition of interferon-beta productionAngela Corona, Elisa Fanunza, Cristiano Salata, et al.
ACS Medicinal Chemistry Letters|August 25, 2017
N-Acylbenzenesulfonamide Dihydro-1,3,4-oxadiazole Hybrids: Seeking Selectivity toward Carbonic Anhydrase IsoformsGiulia Bianco, Rita Meleddu, Simona Distinto, et al.
ACS Medicinal Chemistry Letters|July 24, 2018
Targeting Tumor Associated Carbonic Anhydrases IX and XII: Highly Isozyme Selective Coumarin and Psoralen InhibitorsClaudia Melis, Simona Distinto, Giulia Bianco, et al.
Bioorganic & Medicinal Chemistry|June 29, 2010
Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitorsFranco Chimenti, Daniela Secci, Adriana Bolasco, et al.
Chemmedchem|May 23, 2014
Design, synthesis, and biological evaluation of 1,3-diarylpropenones as dual inhibitors of HIV-1 reverse transcriptaseRita Meleddu, Valeria Cannas, Simona Distinto, et al.
ACS Medicinal Chemistry Letters|October 23, 2018
Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole BenzensulfonamidesRita Meleddu, Simona Distinto, Filippo Cottiglia, et al.
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